Canonical Allele Identifier: CA4905775

Linked Data

dbSNP Id: rs771996574

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142911997_142912002dup , CM000670.2:g.142911997_142912002dup GRCh38
NC_000008.10:g.143993413_143993418dup , CM000670.1:g.143993413_143993418dup GRCh37
NC_000008.9:g.143990415_143990420dup NCBI36
NG_008374.1:g.10845_10850dup

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1493_1498dup (CYP11B2) MANE Select ENSP00000325822.2:p.Phe499_Arg500insThrPh...
ENST00000522728.5:c.182-1966_182-1961dup (GML) ENSP00000430799.1:n.182-1966_182-1961dup
NM_000498.3:c.1493_1498dup (CYP11B2) MANE Select NP_000489.3:p.Phe499_Arg500insThrPhe
XM_011516877.1:c.1640_1645dup (CYP11B2) XP_011515179.1:p.Phe548_Arg549insThrPhe
XM_011516878.1:c.1571_1576dup (CYP11B2) XP_011515180.1:p.Phe525_Arg526insThrPhe
XM_011516879.1:c.1562_1567dup (CYP11B2) XP_011515181.1:p.Phe522_Arg523insThrPhe
XM_011516970.1:c.215-1966_215-1961dup (GML) XP_011515272.1:n.215-1966_215-1961dup